ADA15 Polyclonal Antibody, 50ul Enzymes Mutations in this gene have

Mutations in this gene have been linked with Li-Fraumeni syndrome

Defects in EIF2B4 are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy

Polymorphisms in this gene have been associated with an increased risk of rheumatoid arthritis

tissue specificity:Expressed chiefly in non-neuronal tissues

ADA15 Polyclonal Antibody, 50ul Enzymes Mutations in this gene haveThe protein encoded by this gene is a member of the ADAM (a disintegrin and metalloproteinase) protein family. ADAM family members are type I transmembrane glycoproteins known to be involved in cell adhesion and proteolytic ectodomain processing of cytokines and adhesion molecules. This protein contains multiple functional domains including a zinc binding metalloprotease domain a disintegrin like domain as well as a EGF like domain. Through its